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Enantioselective C−H Borylation for the Synthesis of Axially Chiral N‐Aryl Phthalimides.
- Source :
- Asian Journal of Organic Chemistry; Feb2023, Vol. 12 Issue 2, p1-6, 6p
- Publication Year :
- 2023
-
Abstract
- Axially chiral compounds with a rotation restricted N−C bond are of great importance in synthetic chemistry, pharmaceuticals, and material sciences. The search for efficient and selective routes for the synthesis of these frameworks is of great interest and importance. We herein disclose an iridium‐catalyzed asymmetric C−H borylation protocol for the enantioselective synthesis of chiral N‐aryl phthalimides. The current method features good compatibility of functional groups, broad substrate scope, and high enantioselectivities. We also demonstrate the synthetic utility on a gram‐scale C−H borylation for diverse C−B bond transformations, including the preparation of a chiral catalyst for asymmetric catalysis. [ABSTRACT FROM AUTHOR]
- Subjects :
- PHTHALIMIDES
BORYLATION
MATERIALS science
CHIRALITY element
FUNCTIONAL groups
Subjects
Details
- Language :
- English
- ISSN :
- 21935807
- Volume :
- 12
- Issue :
- 2
- Database :
- Complementary Index
- Journal :
- Asian Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 161984781
- Full Text :
- https://doi.org/10.1002/ajoc.202200695